20 Results for "

CXCL9

" in MedChemExpress (MCE) Product Catalog:
Products (20)

20 Results for "CXCL9" in MCE Product Catalog:

  • Recombinant Proteins Recommended:
2
2 Cited Publications
Cat. No.: HY-P70008
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rMuC-X-C motif chemokine 9/CXCL9, His; C-X-C motif chemokine 9; Gamma-interferon-induced monokine; Monokine induced by interferon-gamma; MIG; MuMIG; Protein m119; Small-inducible cytokine B9; CXCL9; Mig; Scyb9
Species:  
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1 Cited Publications
Cat. No.: HY-P990255

Target:  

CXCR

Research Areas:  

Inflammation/Immunology Cancer

Anti-Mouse CXCL9/MIG Antibody (MIG-2F5.5) is an anti-mouse CXCL9/MIG IgG monoclonal antibody. Anti-Mouse CXCL9/MIG Antibody (MIG-2F5.5) can reduce tumor infiltration of CD8 + cytotoxic T cells (CTLs). Anti-Mouse CXCL9/MIG Antibody (MIG-2F5.5) can prolong the survival of transplanted hearts. Anti-Mouse CXCL9/MIG Antibody (MIG-2F5.5) can be used for researches on immunology and cancer such as prostate cancer .
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1 Cited Publications
Cat. No.: HY-P7253
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuMIG/CXCL9; C-X-C motif chemokine 9; SCYB9
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Cat. No.: HY-165428
CAS No.: 907206-98-8
Target:  

CXCR Arrestin

Research Areas:  

Inflammation/Immunology

SCH-900875 is an orally active, brain-penetrant and selective CXCR3 receptor inhibitor, which also shows high selectivity over CXCR1 and CXCR2 receptors. SCH-900875 binds to CXCR3, blocking the binding of ligands CXCL9, CXCL10, and CXCL11, inhibiting downstream G protein and β-arrestin signaling pathways to suppress inflammatory cell migration. SCH-900875 is promising for research of autoimmune diseases (rheumatoid arthritis, multiple sclerosis) and inflammatory disorders (psoriasis, inflammatory bowel disease) .
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Cat. No.: HY-N7688
CAS No.: 114420-67-6
Regaloside B is a phenylpropane. Regaloside B can be isolated from Lilium longiflorum. Regaloside B can inhibit the expression of VCAM-1, iNOS, and COX-2, with a p-p65/p-65 ratio. Regaloside B inhibits the mRNA of various chemokines and angiogenic factors (CXCL9, CXCL10, IL8, IDO). Regaloside B has anti-inflammatory activity. Regaloside B can be used for osteogenic differentiation research .
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Cat. No.: HY-RS03396
Research Areas:  

Others

CXCL9 Human Pre-designed siRNA Set A contains three designed siRNAs for CXCL9 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-W505771
CAS No.: 523-59-1
Seselin is an anticancer, antinociceptive, anti-inflammatory and antifungal agent. Seselin is orally active .
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Cat. No.: HY-P991610
Synonyms: Sym025

Research Areas:  

Cancer

S-095029 is a humanized IgG1 monoclonal antibody inhibitor targeting NKG2A. S-095029 significantly attenuates Fc-effector functions, inhibits the interaction with its ligand HLA-E, and increases the antibody-dependent cellular cytotoxicity mediated by other Fc-competent mAbs. S-095029 has a potent antitumor activity with enhancement of killing activity and cytokine secretion (IFNγ, TNF-α and CXCL9) of NK and γδ T-cells in co-culture with cancer cells .
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Cat. No.: HY-P10301
Target:  

CXCR

Research Areas:  

Cancer

CXCL9(74-103) is a derivative peptide of CXCL9 that has a high affinity for glycosaminoglycans (GAGs) and can bind to GAGs. CXCL9(74-103) possesses anti-angiogenic properties, capable of reducing EGF, VEGF165, and FGF-2-mediated angiogenesis processes in vitro, without exhibiting cytotoxicity .
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Cat. No.: HY-167884
CAS No.: 319461-60-4
PF-1367550 is a pan-JAK inhibitor. PF-1367550 can decrease the levels of release of CXCL9, CXCL10 and CXCL11 from primary airway epithelial cells .
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Cat. No.: HY-168971
CAS No.: 1390658-79-3
Synonyms: CP-25
Paeoniflorin-6′-O-benzene sulfonate (CP-25) is the inhibitor for G protein-coupled receptor kinase 2 (GRK2) that inhibits the translocation of GRK2 to the cell membrane, inhibits JAK1/STAT3 signaling pathway. Paeoniflorin-6′-O-benzene sulfonate inhibits IL-17A/CXCL2-induced proliferation of HaCaT. Paeoniflorin-6′-O-benzene sulfonate reduces the levels of inflammatory factors and chemokines such as IL-17A, IL-17F, IFN-γ, TNF-α, IL-22, IL-23, CXCL2, CXCL3 and CXCL9, alleviates Imiquimod (HY-B0180)-induced psoriasis in mouse model .
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Cat. No.: HY-162415
CAS No.: 2760585-35-9
Target:  

c-Fms Apoptosis

Research Areas:  

Cancer

CSF1R-IN-22 (Compound C19) is an orally effective CSF-1R selective inhibitor (IC50<6 nM). CSF1R-IN-22 enhances the secretion of CXCL9 from M2 macrophages, increases CD8 + T cell infiltration. CSF1R-IN-22 boosts anti-tumor immune responses of anti-PD-1, and induces apoptosis in tumor cells. CSF1R-IN-22 can effectively reprogram M2-like TAMs (tumor-associated macrophages) to the M1 phenotype and reshape the TME by inducing the recruitment of CD8 + T cells into tumors and reducing the infiltration of immunosuppressive Tregs and MDSCs .
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Cat. No.: HY-P700553
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: C-X-C motif chemokine 9; HuMIG; MIG; CXCL9; CMK; SCYB9
Species:  
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Cat. No.: HY-P77086
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: C-X-C motif chemokine 9; HuMIG; MIG; CXCL9; CMK; SCYB9
Species:  
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Cat. No.: HY-P72675
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: C-X-C motif chemokine 9; HuMIG; MIG; CXCL9; CMK; SCYB9
Species:  
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Cat. No.: HY-P84505
Synonyms: CMK; MIG; Humig; SCYB9; crg-10

Host:  

Mouse

Application:  

ICC/IF, FC, ELISA, ELISA

Reactivity:  

Human

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Cat. No.: HY-P84505A
Synonyms: CMK; MIG; Humig; SCYB9; crg-10

Host:  

Mouse

Application:  

ICC/IF, FC, ELISA, ELISA

Reactivity:  

Human

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Cat. No.: HY-P700235AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: C-X-C motif chemokine 9; Gamma-interferon-induced monokine; Monokine induced by interferon-gamma; MIG; MuMIG; Protein m119; Small-inducible cytokine B9; CXCL9; Mig; Scyb9
Species:  
Pig
Source:  
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Cat. No.: HY-181877
Target:  

HDAC Adenosine Receptor

Research Areas:  

Cancer

IHCH-3185 is an orally active class I HDAC inhibitor (HDAC1 IC50 =102.9 nM) and A2AR antagonist (A2AR Ki =7.6 nM). IHCH-3185 reverses immune gene silencing by inducing histone acetylation and blocks the adenosine signaling pathway to relieve T-cell suppression. IHCH-3185 exhibits antiproliferative activity, induces cell cycle arrest, and significantly improves the tumor microenvironment. IHCH-3185 reduces the proportion of regulatory T cells, increases the CD8 +/Treg ratio, and upregulates the expression of key factors such as H2-K1, Cxcl9 and Cxcl10. IHCH-3185 shows significant antitumor potential in CT26 and MC38 mouse tumor models and is suitable for related cancer research .
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Cat. No.: HY-P700050AF
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: MIG/CXCL9; C-X-C motif chemokine 9; SCYB9
Species:  
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